Impairment of endothelial progenitor cells function in patient with mustard gas intoxication

祖细胞 医学 功能(生物学) 毒理 药理学 重症监护医学 麻醉 干细胞 生物 细胞生物学
作者
Vahid Siavashi,Hadi Cheraghi,Pirouz Pourmohammad,Parviz Nooshirvani,Sara Abdolahi,Amir Solghani,Seyed Mahdi Nassiri,Tooba Ghazanfari
出处
期刊:Inhalation Toxicology [Taylor & Francis]
卷期号:32 (3): 131-140 被引量:1
标识
DOI:10.1080/08958378.2020.1755396
摘要

Background: Sulfur mustard (SM), also known as mustard gas, was first widely used in the Iraq-Iran. After SM exposure, the most prominent clinical signs are the development of extensive non-healing skin wounds and pulmonary signs, persisting over long time. Since the most frequent complications in SM-intoxicated patients are respiratory and dermatologic lesions, and with respect to the important role of endothelial progenitor cells (EPCs) in the pathophysiology of these lesion, we conducted this study to recognize the potential effects of SM on biological features of EPCs in patients exposed with this gas.Methods: In this study, 30 patients with the history of SM exposure during the Iran-Iraq war (1984-1988), 27 patients with pulmonary signs with no history of SM exposure and 20 healthy participants were included. Cell population and function of EPCs were assessed 4 years post-exposure. For this purpose, circulating EPCs (cEPCs) were harvested and cultivated, then the biological features of these cells, including migratory, proliferative, and tubulogenic activities were analyzed. We also measured serum antioxidants levels and mRNA levels of some proangiogenic factors in EPCs from SM-intoxicated patients.Results: Our results showed lesser number of cEPCs in patients exposed with SM, which was associated with decreased proliferative, migratory, and tubulogenic activity of these cells. Also, we found the lesser serum activity of SOD, GPX and MDA in the SM group than in the healthy control group.Conclusions: SM exposure resulted in decreased proliferation and migration of EPCs, which was associated with decreased tubule formation and angiogenic factors.
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